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Moleculin Requests Authorization from the Polish Government to Advance Annamycin HOUSTON

Key Takeaway: Moleculin Requests Authorization from the Polish Government to Advance Annamycin HOUSTON - October 24, 2017 - Moleculin Biotech, Inc., (NASDAQ: MBRX) ("Moleculin" or the "Company"), a clinical stage pharmaceutical company focused on the development of anti-cancer drug candida

Full Press Release Details

Moleculin Requests Authorization from the Polish
Government to Advance Annamycin
HOUSTON - October 24, 2017 -
Moleculin Biotech, Inc., (NASDAQ: MBRX) ("Moleculin" or the "Company"), a clinical stage pharmaceutical company
focused on the development of anti-cancer drug candidates, some of which are based on license agreements with The University of
Texas System on behalf of the M.D. Anderson Cancer Center, today announced that has submitted its request for Clinical Trial Authorization
("CTA") in Poland which, if allowed, will enable a clinical trial to study Annamycin for the treatment of relapsed
or refractory acute myeloid leukemia ("AML") in Poland. This will be in addition to the previously announced allowance
of its Investigative New Drug filing with the Food & Drug Administration in the US.
"Consistent with our prior guidance,
we have now taken the final step required to expand our Annamycin clinical trial to Poland," commented Walter Klemp, Chairman
and CEO of Moleculin. "Unlike the US, the process for beginning a clinical trial in Poland requires a hospital contract before
a request for CTA can be made. We recently announced the required hospital contract and this announcement now marks the formal
request for Polish approval."
Mr. Klemp continued: "The CTA request
process in Poland normally takes 60 days, so we hope to be enrolling patients there near year-end. Increasing the breadth of clinical
trial sites beyond the US will give Moleculin access to more potential patients, and, hopefully, speed the Phase IIa portion of
About Moleculin Biotech, Inc.
Moleculin Biotech, Inc. is a clinical stage
pharmaceutical company focused on the development of anti-cancer drug candidates, some of which are based on discoveries made at
M.D. Anderson Cancer Center. Our lead product candidate is Annamycin, an anthracycline being studied for the treatment of relapsed
or refractory acute myeloid leukemia, more commonly referred to as AML. We also have two preclinical small molecule portfolios
in development, one of which is focused on the modulation of hard-to-target tumor cell signaling mechanisms and the recruitment
of the patient's own immune system. The other portfolio targets the metabolism of tumors.
For more information about the Company, please visit http://www.moleculin.com.
Forward-Looking Statements
Some of the statements in this release
are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, Section 21E of the Securities Exchange
Act of 1934 and the Private Securities Litigation Reform Act of 1995, which involve risks and uncertainties. Forward-looking statements
in this press release include, without limitation, the ability of Annamycin to demonstrate safety and efficacy in cancer patients
and the ability of Moleculin to receive approval to conduct clinical trials in Poland. These statements relate to future events,
future expectations, plans and prospects. Although Moleculin Biotech believes that the expectations reflected in such forward-looking
statements are reasonable as of the date made, expectations may prove to have been materially different from the results expressed
or implied by such forward-looking statements. Moleculin Biotech has attempted to identify forward-looking statements by terminology
including ''believes,'' ''estimates,'' ''anticipates,'' ''expects,'' ''plans,'' ''projects,'' ''intends,'' ''potential,'' ''may,''
''could,'' ''might,'' ''will,'' ''should,'' ''approximately'' or other words that convey uncertainty of future events or outcomes
to identify these forward-looking statements. These statements are only predictions and involve known and unknown risks, uncertainties,
and other factors, including those discussed under Item 1A. "Risk Factors" in our most recently filed Form 10-K filed
with the Securities and Exchange Commission ("SEC") and updated from time to time in our Form 10-Q filings and in our
other public filings with the SEC. Any forward-looking statements contained in this release speak only as of its date. We
undertake no obligation to update any forward-looking statements contained in this release to reflect events or circumstances occurring
after its date or to reflect the occurrence of unanticipated events.
Joe Dorame, Robert Blum or Joe Diaz
Lytham Partners, LLC
Last updated: Oct 24, 2017